Actively Recruiting

Phase Not Applicable
Age: 20Years - 100Years
All Genders
Healthy Volunteers
NCT03174938

The Swedish BioFINDER 2 Study

Led by Skane University Hospital · Updated on 2026-04-06

2950

Participants Needed

2

Research Sites

1020 weeks

Total Duration

On this page

Sponsors

S

Skane University Hospital

Lead Sponsor

L

Lund University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The Swedish BioFINDER 2 study is a new study that will launch in 2017 and extends the previous cohorts of BioFINDER 1 study (www.biofinder.se). BioFINDER 1 is used e.g. to characterize the role of beta-amyloid pathology in early diagnosis of Alzheimer's disease (AD) using amyloid-PET (18F-Flutemetamol) and Aβ analysis in cerebrospinal fluid samples. The BioFINDER 1 study has resulted in more than 40 publications during the last three years, many in high impact journals, and some the of the results have already had important implications for the diagnostic work-up patients with AD in the clinical routine practice. The original BioFINDER 1 cohort started to include participants in 2008. Since then there has been a rapid development of biochemical and neuroimaging technologies which enable novel ways to the study biological processes involved in Alzheimer's disease in living people. There has also been a growing interest in the earliest stages of AD and other neurodegenerative diseases. With the advent of new tau-PET tracers there is now an opportunity to elucidate the role of tau pathology in the pathogenesis of AD and other tauopathies. The Swedish BioFINDER 2 study has been designed to complement the BioFINDER 1 study and to e.g. address issues regarding the role of tau pathology in different dementias and in preclinical stages of different dementia diseases. Further, the clinical assessments and MRI methods have been further optimized compared to BioFINDER 1. Detailed assessments of motor aspects and dual task performance, which is part of a sub-study named Motor-ACT: "Motor aspects and activities in relation to cognitive decline and brain pathologies, has been added to further optimize assessment of motor function.

CONDITIONS

Official Title

The Swedish BioFINDER 2 Study

Who Can Participate

Age: 20Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be aged between 40 and 100 years depending on the cohort
  • For healthy cohorts: no cognitive symptoms and MMSE score 26 or higher
  • For mild cognitive impairment cohort: referred due to cognitive symptoms, MMSE 24-30, no dementia diagnosis, and abnormal CSF amyloid ratio or clinical suspicion of early neurocognitive disorder
  • For Alzheimer's dementia cohort: referred due to cognitive symptoms, MMSE 12-26, diagnosed with Alzheimer's dementia
  • For other dementias cohort: diagnosed with dementia due to FTD, Parkinson's disease dementia, Lewy body dementia, subcortical vascular dementia, Parkinson's disease, PSP, MSA, CBS, or ALS
  • Speak and understand Swedish well enough to complete study procedures without an interpreter
Not Eligible

You will not qualify if you...

  • Have a significant unstable systemic illness or organ failure, such as terminal cancer, preventing study participation
  • Current significant alcohol or substance misuse
  • Significant neurological or psychiatric illness
  • Refuse lumbar puncture, MRI, or PET scans

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Memory Clinic, Hospital of Ängelholm

Ängelholm, Sweden, SE-262 81

Actively Recruiting

2

Memory Clinic, Skåne University Hospital

Malmö, Sweden, SE-20502

Actively Recruiting

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Research Team

E

Erik Stomrud, MD, PhD

CONTACT

S

Sebastian Palmqvist, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

5

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